Colon Cancer: Gene >> RIPK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41741555:41741555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1782G>T
AA Mutation	p.Gln594His(p.Q594H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41740981:41740981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369156558
CDS Mutation	c.2356G>A
AA Mutation	p.Ala786Thr(p.A786T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41741772:41741772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565C>T
AA Mutation	p.Pro522Leu(p.P522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41743897:41743897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772576388
CDS Mutation	c.1324G>A
AA Mutation	p.Glu442Lys(p.E442K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41741787:41741787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550G>A
AA Mutation	p.Arg517His(p.R517H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41751200:41751200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.His174Tyr(p.H174Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41744014:41744014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760710644
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Cys(p.R403C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41751119:41751119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772901408
CDS Mutation	c.601G>A
AA Mutation	p.Asp201Asn(p.D201N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000352483
Start	41741664:41741664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673T>G
AA Mutation	p.Phe558Cys(p.F558C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41741708:41741708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41744078:41744078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770773216
CDS Mutation	c.1143C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41741699:41741699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754260527
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41746710:41746710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763261232
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41741852:41741852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352483
Start	41741772:41741772(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1565delC
AA Mutation	p.Pro522ArgfsTer90(p.P522Rfs*90)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352483
Start	41743956:41743957(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1264dupG
AA Mutation	p.Val422GlyfsTer19(p.V422Gfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RIPK4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352483
Start	41741900:41741900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000352483
Start	41745863:41745863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976G>T
AA Mutation	p.Glu326Ter(p.E326*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript